Post Market Clinical Follow-up Study for the Amvia/Solvia Pacemaker Family

Status Recruiting

Clinical Trial Summary

The study is designed as an open-label, prospective, international, multicenter, non-randomized study to determine safety and product performance of the CE-marked Amvia/Solvia pacemaker family, including the aATP, CRT AutoAdapt and Early Check features in the setting of a post-market clinical follow-up study.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06018818
Study type	Interventional
Source	Biotronik SE & Co. KG
Contact	Dörte Vossmeyer, Dr.
Phone	+49 30 68905 1306
Email	doerte.vossmeyer@biotronik.com
Status	Recruiting
Phase	N/A
Start date	August 23, 2023
Completion date	May 2025

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